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临床试验/NCT04238780
NCT04238780招募中不适用

Ultrasound Guided Erector Spinae Plane Block Reduces Postoperative Pain Following Laparoscopic Colorectal Operation: A Randomized Controlled Study

Gachon University Gil Medical Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年2月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
numerical rating scale on rest and cough

研究概览

简要总结

The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

详细描述

.The goal of this study is to evaluate the effect of ultrasound guided erector spinae plane block on postoperative pain and quality of recovery after laparoscopic colon surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •aged between 20 and 70 years, with an American Society of Anesthesiologists physical status of 1 or 2, who were scheduled for laparoscopic colorectal operation

排除标准

  • •sensitivity to local anesthetic, bleeding disorders , receiving anticoagulant, body mass index (BMI) over 35/kg/m2 spine or chest wall deformity pregnancy tolerance to opioid analgesics inability to use patient-controlled analgesia (PCA)

研究组 & 干预措施

ESP( Erector Spinae Plane Block)

Active Comparator

After induction parturient in the ESPB underwent bilateral ESPB at the level of T7 using a linear ultrasound (US) transducer.

Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.

干预措施: Erector Spinae Plane Block (Procedure)

ESP( Erector Spinae Plane Block)

Active Comparator

After induction parturient in the ESPB underwent bilateral ESPB at the level of T7 using a linear ultrasound (US) transducer.

Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.

干预措施: Intravenous fentanyl patient control device (Procedure)

control group

Active Comparator

No regional anesthesia technique will be applied to the control group.

Intravenous fentanyl patient control device 24-hour fentanyl consumption will be recorded.

干预措施: Intravenous fentanyl patient control device (Procedure)

结局指标

主要结局

numerical rating scale on rest and cough

时间窗: 24 hours after surgery

In the recovery room, post op 6hours, post op 24 hours

次要结局

  • Quality of Recovery(1day before operation, post op 24 hours)
  • need for analgesics(24 hours after surgery)
  • opioid consumption(24 hours after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jung Ju Choi

assistance professor

Gachon University Gil Medical Center

研究点 (1)

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